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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 71535

47 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
March 10, 2015
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
the Compounder

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

47 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 47

BIEST 66/34: TESTOSTERONE : PROGESTERONE IN OLIVE OIL(Estradiol USP Micronized (ED)/Estriol USP Micronized (E3): Testosterone : Progesterone in Olive Oil) 3mg : 4 mg : 100 mg/mL suspension, Rx only, packaged in a 15 mL glass dropper bottle. The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0182-2016
Recall number
D-0182-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
3 (15mL) bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 12192014:35@1, Exp 6/17/2015; Lot # 02202015:68@46, Exp 8/19/15

Distribution pattern

Nationwide

drug · product 2 of 47

BIEST 80/20 : PROGEST : DHEA : TESTOST (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow): Progesterone USP: Dehydroepiandrosterone Micronized (DHEA): Testosterone Trit ) 2.5 : 25 : 2.5 : 0.1MG TROCHE, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0183-2016
Recall number
D-0183-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
60 troches

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 12312014:91@6, Exp 3/31/2015

Distribution pattern

Nationwide

drug · product 3 of 47

BIEST CP 76/24: DHEA (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow) : Dehydroepiandrosterone Micronized (DHEA) 2.625 MG : 10 MG capsules, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0184-2016
Recall number
D-0184-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
90 capsules

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 12312014:44@4, Exp 12/31/2015

Distribution pattern

Nationwide

drug · product 4 of 47

BIEST CP 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)) 1.25 MG capsules, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0185-2016
Recall number
D-0185-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
240 capsules

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 02182015:78@22, Exp 2/18/2016; Lot # 02182015:98@23, Exp 2/18/2016

Distribution pattern

Nationwide

drug · product 5 of 47

BIEST CP 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)) 2.5 MG capsules, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0186-2016
Recall number
D-0186-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
180 capsules

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01162015:59@13, Exp 1/16/2016

Distribution pattern

Nationwide

drug · product 6 of 47

BIEST TD 50/50 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 2.5 MG/ML transdermal cream, dispensed in 10 mL prefilled syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0187-2016
Recall number
D-0187-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
3 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01232015:03@14, Exp 4/23/2015

Distribution pattern

Nationwide

drug · product 7 of 47

BIEST TD 50/50 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 4.0 MG/ML transdermal cream packaged in 3mL syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0188-2016
Recall number
D-0188-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
5 (3mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 12232014:11@21, Exp 6/21/2015

Distribution pattern

Nationwide

drug · product 8 of 47

BIEST TD 67/33 (Estradiol (E2) TRIT (YELLOW)/Estriol USP Micronized (E3)) W/V (weight /volume) 1.5 MG/ML Transdermal cream, dispensed in 3 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0189-2016
Recall number
D-0189-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
10 (3mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 03022015:71@18, Exp 8/29/2015

Distribution pattern

Nationwide

drug · product 9 of 47

BIEST TD 80/20 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 8 MG/ML transdermal cream, dispensed in 3 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0190-2016
Recall number
D-0190-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
5 (3mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01232015:75@4, Exp 7/22/2015

Distribution pattern

Nationwide

drug · product 10 of 47

BIEST TD 80/20 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 0.25 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0191-2016
Recall number
D-0191-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
6 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01262015:27@46, Exp 8/14/2015

Distribution pattern

Nationwide

drug · product 11 of 47

BIEST TD 80/20 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 12.5 MG/ML 1.25MG/0.1ML Transdermal cream, dispensed in 1 mL prefilled, amber syringes,Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0192-2016
Recall number
D-0192-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
9 (1mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01232015:17@35, Exp 8/11/2015

Distribution pattern

Nationwide

drug · product 12 of 47

BIEST TD 80/20 (estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)) W/V (weight/volume) 2.5MG/ML Transdermal cream, dispensed in a) 3 mL and b) 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0193-2016
Recall number
D-0193-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
30 (3mL) syringes, 9 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

a) Lot # 12162014:22@32, Exp 6/14/2015; Lot # 01122015:42@45, Exp 7/11/2015; b) Lot # 01212015:65@5, Exp 7/20/2015

Distribution pattern

Nationwide

drug · product 13 of 47

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)) W/V (weight/volume) 5 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0194-2016
Recall number
D-0194-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
6 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 02062015:50@2, Exp 8/25/2015

Distribution pattern

Nationwide

drug · product 14 of 47

BIEST TD 80/20 (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow)) W/V(weight/volume) [2977] 6.25MG/ML Transdermal cream, dispensed in 1 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0195-2016
Recall number
D-0195-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
36 (1 mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 12222014:95@21, Exp 6/20/2015

Distribution pattern

Nationwide

drug · product 15 of 47

BIEST TD 80/20 (Estradiol (E2) Trit (yellow) / Estriol USP Micronized (E3)): PROG (Progesterone USP Micronized) W/V 2.5MG:100MG/ML Transdermal cream, dispensed in 3 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0196-2016
Recall number
D-0196-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
15 (3 mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01132015:97@2, Exp 4/13/2015

Distribution pattern

Nationwide

drug · product 16 of 47

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized): DHEA (Dehydroepiandrosterone Micronized) : TESTO (Testosterone Trit) W/V (weight/volume) VERSABASE 2.5: 30 : 2.5 : 0.25 MG/MLTransdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0197-2016
Recall number
D-0197-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
18 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 12112014:43@19, Exp 6/9/2015

Distribution pattern

Nationwide

drug · product 17 of 47

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) : TESTO (Testosterone Trit) W/V (weight/volume) VERSABASE 5.0 : 30 : 2.5 : 0.25 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0198-2016
Recall number
D-0198-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
26 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 12172014:08@24, Exp 6/15/2015

Distribution pattern

Nationwide

drug · product 18 of 47

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) : TESTO (Testosterone Trit) W/V (weight/volume) 2.5 : 20 : 1.25 : 0.25 MG/ML TRANSDERMAL (Cream)Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0199-2016
Recall number
D-0199-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
6 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01132015:45@15, Exp 7/12/2015

Distribution pattern

Nationwide

drug · product 19 of 47

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) : TESTO (Testosterone Trit) W/V (weight/volume) VERSABASE 3: 25: 1.25: 0.25 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0200-2016
Recall number
D-0200-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
12 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01232015:29@51, Exp 7/22/2015

Distribution pattern

Nationwide

drug · product 20 of 47

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) : TESTO (Testosterone Trit) W/V (weight/volume) VERSABASE 6.5 : 30: 1.25: 0.25 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0201-2016
Recall number
D-0201-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
12 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01232015:52@49, Exp 7/22/2015

Distribution pattern

Nationwide

drug · product 21 of 47

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) IN VERSABASE W/V (weight/volume) 2.5 : 25 :1.25MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0202-2016
Recall number
D-0202-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
66 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 02022015:66@40, Exp 8/1/2015; Lot # 03022015:62@26, Exp 8/29/2015; Lot # 03062015:66@10, Exp by 9/2/2015

Distribution pattern

Nationwide

drug · product 22 of 47

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) IN VERSABASE W/V (weight/volume) 4 : 67.5 :10MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0203-2016
Recall number
D-0203-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
18 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 02252015:80@18, Exp 8/24/2015

Distribution pattern

Nationwide

drug · product 23 of 47

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : TESTO (Testosterone USP) : DHEA (Dehydroepiandrosterone Micronized) W/V (weight/volume) VERSABASE 2.5 : 17.5 : 1.25 :0.25MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only,The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0204-2016
Recall number
D-0204-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
12 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01152015:68@24, Exp 7/14/2015; and Lot # 02192015:15@12, Exp 8/18/2015

Distribution pattern

Nationwide

drug · product 24 of 47

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : TESTO (Testosterone USP) W/V (weight/volume) 5.0 :20 :1 MG/ML Transdermal cream, dispensed in 5 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0205-2016
Recall number
D-0205-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
15 (5mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01122015:21@8, Exp 7/11/2015; Lot # 02092015:09@4, Exp 8/8/2015; Lot # 03092015:66@35, Exp 9/5/2015

Distribution pattern

Nationwide

drug · product 25 of 47

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : TESTO (Testosterone USP) W/V (weight/volume) 1.25:100:0.625 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only,The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0206-2016
Recall number
D-0206-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
12 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01122015:25@6, Exp 7/11/2015; Lot # 03042015:64@14, Exp 8/31/2015

Distribution pattern

Nationwide

drug · product 26 of 47

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : TESTO (Testosterone USP) W/V (weight/volume) 1.0 :4.0 MG/ML Transdermal cream, dispensed in 3 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0207-2016
Recall number
D-0207-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
5 (3mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01052015:78@27, Exp 7/4/2015

Distribution pattern

Nationwide

drug · product 27 of 47

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) VAN CR (vanishing cream) W/V (weight/volume) (4812) 2.5MG/ML Transdermal cream, dispensed in a) 1mL and b)3 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0208-2016
Recall number
D-0208-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
1(1mL) syringe, 56 (3mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

a) Lot # 12292014:90@21, Exp 6/27/2015; b) Lot # 02032015:55@13, Exp 8/2/2015

Distribution pattern

Nationwide

drug · product 28 of 47

BIEST TD 83/17 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) W/V (weight/volume) 1.2 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0209-2016
Recall number
D-0209-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
6 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01052015:05@12, Exp 7/4/2015

Distribution pattern

Nationwide

drug · product 29 of 47

BIEST TD 86/14 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) IN PLO GEL (Pluronic F127 20% or Polox 20% gel) 2.9 MG/ML Transdermal cream, dispensed in 3 mL prefilled, amber syringes, Rx only,The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0210-2016
Recall number
D-0210-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
20 (3mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 12102014:93@49, Exp 6/8/2015

Distribution pattern

Nationwide

drug · product 30 of 47

BIEST TD 89/11 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) W/V (weight/volume) VERSABASE 2.25MG/ML Transdermal cream, dispensed in 3 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0211-2016
Recall number
D-0211-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
10 (3mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 02182015:05@17, Exp 8/17/2015

Distribution pattern

Nationwide

drug · product 31 of 47

BIEST TD 91/9 (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow)) : PROGESTERONE W/V (weight/volume) PLO (Pluronic F127 20% or Polox 20% gel) 3.3 MG/ML : 40 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0212-2016
Recall number
D-0212-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
10 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 12242014:95@3, Exp 6/22/2015; Lot # 02042015:29@7; Exp 8/3/2015

Distribution pattern

Nationwide

drug · product 32 of 47

E2 (Estradiol (E2) Trit (Yellow) : E3 (Estriol USP Micronized (E3) : PROGEST (Progesterone USP Micronized) : TESTOST (Testosterone USP) IN OLIVE OIL 0.75 : 3 : 50 : 5MG capsules, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0213-2016
Recall number
D-0213-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
120 capsules

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 02172015:64@24, Exp 5/18/2015

Distribution pattern

Nationwide

drug · product 33 of 47

ESTRIOL (E3) 4.0MG capsules, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0214-2016
Recall number
D-0214-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
90 capsules

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01142015:26@28, Exp 1/14/2016

Distribution pattern

Nationwide

drug · product 34 of 47

ESTRIOL (E3) : PROGESTERONE : DHEA (Dehydroepiandrosterone Micronized) W/V (weight/volume) VERSABASE 4.0 : 30 : 4MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0215-2016
Recall number
D-0215-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
3 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01282015:71@21, Exp 7/27/2015

Distribution pattern

Nationwide

drug · product 35 of 47

ESTRIOL (E3) : PROGESTERONE W/V (weight/volume) 4.0 : 100 MG/ML Transdermal cream, dispensed in 3 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0216-2016
Recall number
D-0216-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
40 (3mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 12172014:36@7, Exp 6/15/2015; Lot # 02202015:63@45, Exp 8/19/2015

Distribution pattern

Nationwide

drug · product 36 of 47

ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : PROGEST (Progesterone USP) : TESTO (Testosterone USP) W/V (weight/volume) 2 :0.1 : 35 : 0.5 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0217-2016
Recall number
D-0217-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
6 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01132015:27@20, Exp 7/12/2015

Distribution pattern

Nationwide

drug · product 37 of 47

ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : PROGEST (Progesterone USP) : TESTO (Testosterone USP) W/V (weight/volume) 2 :0.1 : 30 : 0.5 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0218-2016
Recall number
D-0218-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
5 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01162015:90@26, Exp 7/15/2015

Distribution pattern

Nationwide

drug · product 38 of 47

ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : TESTO (Testosterone USP) W/V (weight/volume) 2.0: 0.1: 0.5MG/ML Transdermal cream, dispensed in 5 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0219-2016
Recall number
D-0219-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
9 (5mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 12102014:82@10, Exp 6/8/2015

Distribution pattern

Nationwide

drug · product 39 of 47

ESTRIOL (E3) : TESTO (Testosterone USP) WV (weight/volume) 0.5MG : 2MG/ML Transdermal cream, dispensed in 3 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0220-2016
Recall number
D-0220-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
30 (3mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 12292014:45@12, Exp 6/27/2015; Lot # 01282015:06@16, Exp 7/27/2015; Lot # 03022015:06@38, Exp 8/29/2015

Distribution pattern

Nationwide

drug · product 40 of 47

ESTRIOL (E3) 2.5MG suppositories, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0221-2016
Recall number
D-0221-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
20 suppositories

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01132015:97@2, Exp 4/13/2015

Distribution pattern

Nationwide

drug · product 41 of 47

ESTRIOL (E3) W/V (weight/volume) PGF 0.1% (1.0MG/ML) Transdermal cream, is dispensed in 3 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0222-2016
Recall number
D-0222-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
10 (3mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 12302014:27@3; use by 6/28/2015; and Lot # 02252015:26@3; use by 8/24/2015

Distribution pattern

Nationwide

drug · product 42 of 47

ESTRIOL (E3) W/V (weight/volume) VERSABASE 3MG/ML Transdermal cream, dispensed in 5 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0223-2016
Recall number
D-0223-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
6 (5mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01232015:87@5, Exp 7/22/2015

Distribution pattern

Nationwide

drug · product 43 of 47

ESTRIOL (E3) W/V (weight/volume) VERSABASE [4714] 0.05% (0.5MG/ML) transdermal cream, dispensed in a) 1 mL and b) 3 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0224-2016
Recall number
D-0224-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
10 (3mL) syringes, 20 (1mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

a) Lot # 12292014:32@20, Exp 6/27/2015; b) Lot # 01082015:73@21, Exp 7/7/2015

Distribution pattern

Nationwide

drug · product 44 of 47

ESTRIOL 5 ESTRADIOL (Estradiol (E2) Trit (Yellow)) 0.95 ESTRONE (Estrone E1) Trit (Red)) 0.02 TEST (Testosterone USP) 0.75MG/ML W/V (weight/volume) transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0225-2016
Recall number
D-0225-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
20 (10mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 12182014:10@21, Exp 6/16/2015; Lot # 01292015:64@13, Exp 7/28/2015

Distribution pattern

Nationwide

drug · product 45 of 47

TRIEST 70/20/10 ( Estriol USP / Estradiol USP (E2) / Estrone (E1) Triturate) [909] 12.5MG/ML transdermal cream, dispensed in 1 mL prefilled amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0226-2016
Recall number
D-0226-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
24 (1mL) syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 12222014:81@25, Exp 6/20/2015

Distribution pattern

Nationwide

drug · product 46 of 47

TRIEST 80/10/10 (E1/E2 Trit - Estrone (E1)/Estradiol (E2) / Estriol USP (E3)) (23) 5MG capsules, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0227-2016
Recall number
D-0227-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
120 capsules

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 12302014:78@17, Exp 12/30/2015, Lot # 03032015:04@4, Exp 3/2/2016

Distribution pattern

Nationwide

drug · product 47 of 47

TRIEST 80/10/10 (Estrone (E1) Trit / Estradiol (E2) Trit / Estriol USP (E3)) 1.875MG capsules, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

D-0228-2016
Recall number
D-0228-2016
Initiated
March 10, 2015
Classification
Class II
Status
Terminated
Recalling firm
the Compounder
Quantity
60 capsules

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Code information

Lot # 01222015:18@3, Exp 7/21/2015

Distribution pattern

Nationwide